000 04053cam a2200769Ia 4500
001 ocn829279532
003 OCoLC
005 20171107091919.0
006 m o d
007 cr cnu|||unuuu
008 130307s2013 enka ob 001 0 eng d
020 _a9783527656714
020 _a3527656715
020 _a9783527656745
020 _a352765674X
020 _a9783527656738
020 _a3527656731
020 _a9783527656721
020 _a3527656723
020 _z9783527332052
020 _z3527332057
020 _z352765674X
020 _z9783527656738
020 _z3527656731
020 _z9783527656721
020 _z3527656723
020 _z9781299402140
020 _z1299402143
029 1 _aAU@
_b000050718468
029 1 _aAU@
_b000053032919
029 1 _aCHBIS
_b010131840
029 1 _aCHVBK
_b314711643
029 1 _aDEBBG
_bBV041390113
029 1 _aDEBSZ
_b431350159
029 1 _aDKDLA
_b820120-katalog:000651725
029 1 _aNZ1
_b15340118
035 _a(OCoLC)829279532
_z(OCoLC)837185854
_z(OCoLC)961570972
_z(OCoLC)962651904
037 _a471464
_bMIL
040 _aDG1
_beng
_epn
_cDG1
_dEBLCP
_dMHW
_dYDXCP
_dCOO
_dCDX
_dOCLCO
_dIDEBK
_dN$T
_dIUL
_dE7B
_dNOC
_dHEBIS
_dOCLCO
_dOCLCF
_dOCLCQ
_dDEBSZ
_dOCLCQ
049 _aMAIN
050 4 _aQD281.C7
_bM63 2013
072 7 _aSCI
_2eflch
072 7 _aSCI
_x013040
_2bisacsh
082 0 4 _a547.036
_223
245 0 0 _aModern methods in stereoselective aldol reactions /
_cedited by Rainer Mahrwald.
_h[electronic resource]
260 _aWeinheim :
_bWiley-VCH,
_c©2013.
300 _a1 online resource (xiv, 536 pages) :
_billustrations
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
504 _aIncludes bibliographical references and index.
505 0 _aStereoselective Acetate Aldol Reactions / Pedro Romea, Fèlix Urpí -- The Vinylogous Mukaiyama Aldol Reaction in Natural Product Synthesis / Martin Cordes, Markus Kalesse -- Organocatalyzed Aldol Reactions / Gabriela Guillena -- Supersilyl Protective Groups in Aldol Reactions / Patrick B Brady, Hisashi Yamamoto -- Asymmetric Induction in Aldol Additions / Luiz C Dias, Ellen C Polo, Emílio C de Lucca, Marco A B Ferreira -- Polypropionate Synthesis via Substrate-Controlled Stereoselective Aldol Couplings of Chiral Fragments / Dale E Ward -- Application of Oxazolidinethiones and Thiazolidinethiones in Aldol Additions / Michael T Crimmins -- Enzyme-Catalyzed Aldol Additions / Pere Clapés, Jesús Joglar.
520 _aThis sequel to the highly successful and much appreciated "Modern Aldol Reactions" continues to provide a systematic overview of methodologies for installing a required configuration during an aldol addition step, but shifts the focus so as to cover the latest developments. As such, it presents a set of brand new tools, including vinylogous Mukaiyama-aldol reactions, substrate-controlled aldol reactions and asymmetric induction in aldol additions. Furthermore, novel developments in existing stereoselective aldol additions are described, such as the deployment of supersilyl groups or organocatalyzed aldol additions. Throughout, all of these methodologies are presented in the context of their deployment in total synthesis of natural products.
588 0 _aPrint version record.
650 0 _aAldol condensation.
650 0 _aAldehydes.
650 7 _aSCIENCE
_xChemistry
_xOrganic.
_2bisacsh
650 7 _aAldehydes.
_2fast
_0(OCoLC)fst00804652
650 7 _aAldol condensation.
_2fast
_0(OCoLC)fst00804678
650 7 _aAldolreaktion
_2gnd
_0(DE-588)4324196-7
650 7 _aStereoselektive Reaktion
_2gnd
_0(DE-588)4132164-9
655 4 _aElectronic books.
700 1 _aMahrwald, Rainer,
_d1950-
776 0 8 _iPrint version:
_tModern methods in stereoselective aldol reactions.
_dWeinheim : Wiley-VCH, ©2013
_z9783527332052
_w(OCoLC)827785572
856 4 0 _uhttp://onlinelibrary.wiley.com/book/10.1002/9783527656714
_zWiley Online Library
942 _2ddc
_cBK
999 _c206558
_d206558